Letteboer TG - Search Results

1

[Diagnosis of fetal alcohol spectrum disorders].

van Wieringen H, Letteboer TG, Pereira RR, de Ruiter S, Balemans WA, Lindhout D. van Wieringen H, et al. Among authors: letteboer tg. Ned Tijdschr Geneeskd. 2010;154:A331. Ned Tijdschr Geneeskd. 2010. PMID: 20858301 Review. Dutch.

2

Genotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia.

Letteboer TG, Mager HJ, Snijder RJ, Lindhout D, Ploos van Amstel HK, Zanen P, Westermann KJ. Letteboer TG, et al. Am J Med Genet A. 2008 Nov 1;146A(21):2733-9. doi: 10.1002/ajmg.a.32243. Am J Med Genet A. 2008. PMID: 18831062

3

Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients.

Letteboer TG, Zewald RA, Kamping EJ, de Haas G, Mager JJ, Snijder RJ, Lindhout D, Hennekam FA, Westermann CJ, Ploos van Amstel JK. Letteboer TG, et al. Hum Genet. 2005 Jan;116(1-2):8-16. doi: 10.1007/s00439-004-1196-5. Epub 2004 Oct 23. Hum Genet. 2005. PMID: 15517393

4

Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia.

Letteboer TG, Mager JJ, Snijder RJ, Koeleman BP, Lindhout D, Ploos van Amstel JK, Westermann CJ. Letteboer TG, et al. J Med Genet. 2006 Apr;43(4):371-7. doi: 10.1136/jmg.2005.035451. Epub 2005 Sep 9. J Med Genet. 2006. PMID: 16155196 Free PMC article.

5

A pulmonary right-to-left shunt in patients with hereditary hemorrhagic telangiectasia is associated with an increased prevalence of migraine.

Post MC, Letteboer TG, Mager JJ, Plokker TH, Kelder JC, Westermann CJ. Post MC, et al. Among authors: letteboer tg. Chest. 2005 Oct;128(4):2485-9. doi: 10.1378/chest.128.4.2485. Chest. 2005. PMID: 16236913

6

Hereditary hemorrhagic telangiectasia: how accurate are the clinical criteria?

van Gent MW, Velthuis S, Post MC, Snijder RJ, Westermann CJ, Letteboer TG, Mager JJ. van Gent MW, et al. Among authors: letteboer tg. Am J Med Genet A. 2013 Mar;161A(3):461-6. doi: 10.1002/ajmg.a.35715. Epub 2013 Feb 8. Am J Med Genet A. 2013. PMID: 23401183

7

Assessment of intestinal vascular malformations in patients with hereditary hemorrhagic teleangiectasia and anemia.

van Tuyl SA, Letteboer TG, Rogge-Wolf C, Kuipers EJ, Snijder RJ, Westermann CJ, Stolk MF. van Tuyl SA, et al. Among authors: letteboer tg. Eur J Gastroenterol Hepatol. 2007 Feb;19(2):153-8. doi: 10.1097/01.meg.0000252633.88419.04. Eur J Gastroenterol Hepatol. 2007. PMID: 17273001

8

SMAD4 mutations found in unselected HHT patients.

Gallione CJ, Richards JA, Letteboer TG, Rushlow D, Prigoda NL, Leedom TP, Ganguly A, Castells A, Ploos van Amstel JK, Westermann CJ, Pyeritz RE, Marchuk DA. Gallione CJ, et al. Among authors: letteboer tg. J Med Genet. 2006 Oct;43(10):793-7. doi: 10.1136/jmg.2006.041517. Epub 2006 Apr 13. J Med Genet. 2006. PMID: 16613914 Free PMC article.

9

Is hereditary haemorrhagic telangiectasia rare in the black race? The first sub-Saharan mutation.

Westermann CJ, Kitonyi GW, Letteboer TG. Westermann CJ, et al. Among authors: letteboer tg. Haemophilia. 2011 Jan;17(1):e244. doi: 10.1111/j.1365-2516.2010.02353.x. Haemophilia. 2011. PMID: 20609011 No abstract available.

10

Genetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformation in hereditary hemorrhagic telangiectasia 1 (HHT1) and may influence expression of PTPN14.

Letteboer TG, Benzinou M, Merrick CB, Quigley DA, Zhau K, Kim IJ, To MD, Jablons DM, van Amstel JK, Westermann CJ, Giraud S, Dupuis-Girod S, Lesca G, Berg JH, Balmain A, Akhurst RJ. Letteboer TG, et al. Front Genet. 2015 Mar 12;6:67. doi: 10.3389/fgene.2015.00067. eCollection 2015. Front Genet. 2015. PMID: 25815003 Free PMC article.

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